chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	228661637	228661638	T	C	1	GENIC	homozygous	61107344
1	228661888	228661889	G	C	30	GENIC	homozygous	61107345
1	228662090	228662091	C	T	30	GENIC	possibly homozygous	61927696
1	228662170	228662171	G	A	29	GENIC	possibly homozygous	61107346
1	228663365	228663366	G	A	24	GENIC	possibly homozygous	61927698
1	228665193	228665194	T	C	16	GENIC	homozygous	61107350
1	228669156	228669157	C	T	25	GENIC	homozygous	61927699
1	228669606	228669607	G	A	7	GENIC	heterozygous	61107352
1	228669631	228669632	T	C	7	GENIC	homozygous	61107353
1	228670146	228670147	A	G	16	GENIC	homozygous	61107354
1	228670265	228670266	C	T	27	GENIC	possibly homozygous	61927700
1	228671386	228671387	G	A	14	GENIC	possibly homozygous	61107355
1	228672902	228672903	G	T	5	GENIC	homozygous	61927701
1	228673616	228673617	C	T	15	GENIC	homozygous	61107357
1	228675201	228675202	T	C	22	GENIC	possibly homozygous	61107358
1	228675312	228675313	C	T	29	GENIC	possibly homozygous	61107359
1	228675602	228675603	T	C	30	GENIC	homozygous	61927702
1	228676534	228676535	G	T	22	GENIC	homozygous	61107362
1	228676585	228676586	C	CT	1	GENIC	homozygous	61107363
1	228678104	228678105	A	G	3	GENIC	homozygous	61107366
1	228678861	228678862	G	C	13	GENIC	homozygous	61927703
1	228680073	228680074	C	T	22	GENIC	possibly homozygous	61107369